Literature DB >> 3036630

Different molecular mechanisms for cAMP regulation of gene expression during Dictyostelium development.

A R Kimmel.   

Abstract

Alterations in cAMP concentrations have been implicated in developmentally regulated gene expression in Dictyostelium. Using a variety of culture conditions to control the metabolism of cAMP during cytodifferentiation, I have examined the role of the cyclic nucleotide in development. Conditions which allow intracellular synthesis of cAMP promote the normal developmental repression of gene M4-1 by a mechanism which is completely independent of the formation of multicellular aggregates. If, however, cells are inhibited in their ability to activate adenylate cyclase and, thus, intracellular cAMP signaling, they prove unable to repress M4-1, even in the presence of exogenous cAMP. In contrast, expression of genes which exhibit maximal activity after aggregate formation depends upon accumulation of extracellular cAMP. Inhibition of intracellular cAMP signaling does not prevent the expression of these genes if cultures are simultaneously exposed to high levels of exogenously added extracellular cAMP. These results indicate that there are at least two independent mechanisms involved in the developmental regulation of gene expression by cAMP in Dictyostelium. I discuss plausible molecular mechanisms through which cAMP might alter gene expression.

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Year:  1987        PMID: 3036630     DOI: 10.1016/0012-1606(87)90342-3

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  30 in total

1.  Constitutively active G protein-coupled receptor mutants block dictyostelium development.

Authors:  Minghang Zhang; Mousumi Goswami; Dale Hereld
Journal:  Mol Biol Cell       Date:  2004-12-01       Impact factor: 4.138

2.  Disruption of the gene encoding the p34/31 polypeptides affects growth and development of Dictyostelium discoideum.

Authors:  G Bain; A Tsang
Journal:  Mol Gen Genet       Date:  1991-04

3.  Identification of Dictyostelium G alpha genes expressed during multicellular development.

Authors:  J A Hadwiger; T M Wilkie; M Strathmann; R A Firtel
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

4.  SAS1 and SAS2, GTP-binding protein genes in Dictyostelium discoideum with sequence similarities to essential genes in Saccharomyces cerevisiae.

Authors:  S A Saxe; A R Kimmel
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

5.  Regulation of the Discoidin I gamma gene in Dictyostelium discoideum: identification of individual promoter elements mediating induction of transcription and repression by cyclic AMP.

Authors:  F Vauti; P Morandini; J Blusch; A Sachse; W Nellen
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

6.  Autonomous and nonautonomous regulation of axis formation by antagonistic signaling via 7-span cAMP receptors and GSK3 in Dictyostelium.

Authors:  G T Ginsburg; A R Kimmel
Journal:  Genes Dev       Date:  1997-08-15       Impact factor: 11.361

7.  Expression and organization of BP74, a cyclic AMP-regulated gene expressed during Dictyostelium discoideum development.

Authors:  S B Hopkinson; R S Pollenz; I Drummond; R L Chisholm
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

8.  Identification of a signal transduction response sequence element necessary for induction of a Dictyostelium discoideum gene by extracellular cyclic AMP.

Authors:  J Pavlovic; B Haribabu; R P Dottin
Journal:  Mol Cell Biol       Date:  1989-11       Impact factor: 4.272

9.  Inositol trisphosphate and diacylglycerol can differentially modulate gene expression in Dictyostelium.

Authors:  G Ginsburg; A R Kimmel
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

10.  Amino acid substitutions in the Dictyostelium G alpha subunit G alpha 2 produce dominant negative phenotypes and inhibit the activation of adenylyl cyclase, guanylyl cyclase, and phospholipase C.

Authors:  K Okaichi; A B Cubitt; G S Pitt; R A Firtel
Journal:  Mol Biol Cell       Date:  1992-07       Impact factor: 4.138

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